ATP9B
ATPase phospholipid transporting 9B
Summary
Predicted to enable ATPase-coupled intramembrane lipid transporter activity. Predicted to be involved in endocytosis; phospholipid translocation; and retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum. Located in perinuclear region of cytoplasm and trans-Golgi network. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants92 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1035000530 | 18:76,829,417 | G/T | — | uncertain significance |
| rs376573401 | 18:76,829,424 | T/G | — | uncertain significance |
| rs747144142 | 18:76,829,427 | C/T | — | uncertain significance |
| rs762690907 | 18:76,829,436 | C/T | — | uncertain significance |
| rs529205323 | 18:76,829,441 | C/T | — | uncertain significance |
| rs765747731 | 18:76,829,450 | G/C | — | uncertain significance |
| rs141384028 | 18:76,829,458 | C/T | — | likely benign |
| rs911658150 | 18:76,829,475 | G/T | — | uncertain significance |
| rs746138437 | 18:76,829,481 | C/T | — | uncertain significance |
| rs749089234 | 18:76,829,490 | G/T | — | uncertain significance |
| rs1219708995 | 18:76,829,519 | C/T | — | uncertain significance |
| rs181100780 | 18:76,856,499 | C/T | — | uncertain significance |
| rs148439063 | 18:76,856,502 | A/T | — | uncertain significance |
| rs368760695 | 18:76,856,537 | G/C | — | uncertain significance |
| rs372679952 | 18:76,856,549 | G/A | — | uncertain significance |
| rs199859397 | 18:76,856,577 | G/A | — | uncertain significance |
| rs144519079 | 18:76,856,627 | G/A | — | uncertain significance |
| rs777060597 | 18:76,870,371 | A/G | — | likely benign |
| rs763076944 | 18:76,870,408 | G/A | — | uncertain significance |
| rs751763607 | 18:76,870,410 | A/C | — | uncertain significance |
| rs761759241 | 18:76,870,411 | C/T | — | uncertain significance |
| rs617472 | 18:76,870,412 | A/C | — | benign |
| rs145161958 | 18:76,873,346 | G/A | — | uncertain significance |
| rs753284976 | 18:76,886,294 | C/T | — | uncertain significance |
| rs758807274 | 18:76,886,295 | G/A | — | uncertain significance |
| rs148387710 | 18:76,886,319 | G/A | — | uncertain significance |
| rs773068417 | 18:76,886,328 | G/A | — | uncertain significance |
| rs137963592 | 18:76,903,852 | G/A | — | uncertain significance |
| rs200187731 | 18:76,914,520 | C/T | — | uncertain significance |
| rs1568338113 | 18:76,936,863 | C/G | — | uncertain significance |
| rs2513444496 | 18:76,936,873 | C/T | — | uncertain significance |
| rs147426701 | 18:76,953,231 | G/A | — | uncertain significance |
| rs185631368 | 18:76,953,262 | G/A | — | uncertain significance |
| rs776529294 | 18:76,973,982 | A/C | — | uncertain significance |
| rs750643865 | 18:76,973,988 | A/G | — | uncertain significance |
| rs201221449 | 18:77,013,409 | G/A | — | likely benign |
| rs1113034 | 18:77,013,425 | A/G | — | benign |
| rs2096050596 | 18:77,013,498 | C/T | — | uncertain significance |
| rs149013492 | 18:77,037,059 | G/A | — | uncertain significance |
| rs749938619 | 18:77,037,097 | A/G | — | uncertain significance |
| rs775197791 | 18:77,063,637 | G/A | — | uncertain significance |
| rs142685265 | 18:77,063,668 | C/T | — | likely benign |
| rs768374404 | 18:77,063,675 | A/G | — | uncertain significance |
| rs36034863 | 18:77,063,702 | G/A | — | benign |
| rs139181346 | 18:77,066,999 | C/A | — | likely benign |
| rs34750827 | 18:77,067,143 | G/A | — | likely benign |
| rs34339254 | 18:77,067,171 | C/T | — | benign |
| rs551659252 | 18:77,067,203 | A/G | — | uncertain significance |
| rs778281431 | 18:77,089,141 | G/A | — | uncertain significance |
| rs142521017 | 18:77,089,144 | G/A | — | uncertain significance |
| rs35782512 | 18:77,089,273 | G/A | — | uncertain significance |
| rs149979572 | 18:77,089,297 | G/A | — | uncertain significance |
| rs758180960 | 18:77,090,057 | G/A | — | uncertain significance |
| rs769469626 | 18:77,090,075 | G/A | — | uncertain significance |
| rs112066680 | 18:77,090,219 | A/G | intron variant | — |
| rs748739665 | 18:77,096,655 | C/T | — | uncertain significance |
| rs201172611 | 18:77,096,664 | G/A | — | uncertain significance |
| rs775555401 | 18:77,096,686 | C/T | — | uncertain significance |
| rs115068761 | 18:77,096,714 | G/A | — | benign |
| rs778892366 | 18:77,097,321 | C/T | — | uncertain significance |
| rs140060049 | 18:77,097,333 | G/A | — | uncertain significance |
| rs149798512 | 18:77,097,334 | C/T | — | uncertain significance |
| rs2516524923 | 18:77,097,392 | C/A | — | uncertain significance |
| rs754192607 | 18:77,097,396 | C/A | — | uncertain significance |
| rs976628308 | 18:77,097,432 | C/T | — | uncertain significance |
| rs554790401 | 18:77,097,438 | G/A | — | uncertain significance |
| rs62096820 | 18:77,100,108 | G/C | — | — |
| rs142654821 | 18:77,104,269 | C/A | — | uncertain significance |
| rs778867446 | 18:77,104,274 | C/T | — | uncertain significance |
| rs944660957 | 18:77,104,283 | G/C | — | uncertain significance |
| rs2096874170 | 18:77,104,290 | T/C | — | uncertain significance |
| rs371521589 | 18:77,104,361 | C/G | — | likely benign |
| rs1306031130 | 18:77,105,463 | G/C | — | uncertain significance |
| rs772299729 | 18:77,105,497 | C/T | — | uncertain significance |
| rs776703909 | 18:77,105,510 | C/T | — | uncertain significance |
| rs372879560 | 18:77,105,522 | G/T | — | uncertain significance |
| rs926575952 | 18:77,105,558 | G/A | — | uncertain significance |
| rs2096883016 | 18:77,105,828 | A/T | — | uncertain significance |
| rs1270690372 | 18:77,105,829 | T/C | — | uncertain significance |
| rs374039124 | 18:77,107,783 | C/T | — | uncertain significance |
| rs765265533 | 18:77,108,186 | C/T | — | uncertain significance |
| rs371117673 | 18:77,119,421 | A/G | — | uncertain significance |
| rs1304072135 | 18:77,119,437 | C/T | — | uncertain significance |
| rs149975826 | 18:77,133,899 | C/T | — | likely benign |
| rs2517238229 | 18:77,133,927 | C/G | — | uncertain significance |
| rs1405034049 | 18:77,133,951 | G/A | — | uncertain significance |
| rs140981029 | 18:77,133,958 | C/T | — | uncertain significance |
| rs377352041 | 18:77,133,972 | G/A | — | uncertain significance |
| rs2517241392 | 18:77,134,039 | T/C | — | uncertain significance |
| rs772344558 | 18:77,134,080 | G/A | — | uncertain significance |
| rs1253018878 | 18:77,137,278 | G/A | — | likely benign |
| rs150079485 | 18:77,137,343 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.